1 Department of Clinical Dentistry, Centre for Clinical Dental Research, University of Bergen , Bergen, Norway .
2 Department of Periodontology, Faculty of Odontology, Malmö University , Malmö, Sweden .
Tissue Eng Part B Rev. 2017 Dec;23(6):552-569. doi: 10.1089/ten.TEB.2017.0093. Epub 2017 Jul 28.
Fetal bovine serum (FBS) is the most commonly used supplement for ex vivo expansion of human mesenchymal stem cells (hMSCs) for bone tissue engineering applications. However, from a clinical standpoint, it is important to substitute animal-derived products according to current good manufacturing practice (cGMP) guidelines. Humanized alternatives to FBS include three categories of products: human serum (HS), human platelet derivatives (HPDs)-including platelet lysate (PL) or platelet releasate (PR), produced by freeze/thawing or chemical activation of platelet concentrates, respectively, and chemically defined media (serum-free) (CDM). In this systematic literature review, the in vitro and in vivo osteogenic potential of hMSCs expanded in humanized (HS-, HPD-, or CDM-supplemented) media versus hMSCs expanded in FBS-supplemented media, was compared. In addition, PL and PR were compared in terms of their growth factor (GF)/cytokine-content and cell-culture efficacy. When using either 10-20% autologous or pooled HS, 3-10% pooled HPDs or CDM supplemented with GFs, in comparison with 10-20% FBS, a majority of studies reported similar or superior in vitro proliferation and osteogenic differentiation, and in vivo bone formation in ectopic or orthotopic rodent models. Moreover, a trend for higher GF content was observed in PL versus PR, although evidence for cell culture efficacy is limited. In summary, humanized supplements seem at least equally effective as FBS for hMSC expansion and osteogenic differentiation. Although pooled HPDs appear to be the most favorable supplement for large-scale hMSC expansion, further efforts are needed to standardize the preparation and composition of these products in compliance with cGMP standards.
胎牛血清(FBS)是体外扩增人骨髓间充质干细胞(hMSC)用于骨组织工程应用最常用的补充剂。然而,从临床角度来看,根据现行良好生产规范(cGMP)指南,用动物源性产品替代 FBS 非常重要。FBS 的人源替代品包括以下三类产品:人血清(HS)、人血小板衍生物(HPD),包括血小板裂解液(PL)或血小板释放液(PR),分别通过血小板浓缩物的冻融或化学激活产生,以及化学成分确定的培养基(无血清)(CDM)。在这项系统文献综述中,比较了在人源化(HS-、HPD-或 CDM 补充)培养基中扩增的 hMSC 与在 FBS 补充培养基中扩增的 hMSC 的体外和体内成骨潜能。此外,还比较了 PL 和 PR 在生长因子(GF)/细胞因子含量和细胞培养功效方面的差异。当使用 10-20%自体或混合 HS、3-10%混合 HPD 或 CDM 补充 GF 与 10-20% FBS 相比,大多数研究报告称,在体外增殖和成骨分化以及异位或原位啮齿动物模型中的体内骨形成方面,类似或更优。此外,PL 中的 GF 含量高于 PR,但细胞培养功效的证据有限。总之,人源化补充剂至少与 FBS 一样有效,可用于 hMSC 的扩增和成骨分化。虽然混合 HPD 似乎是大规模 hMSC 扩增最有利的补充剂,但仍需要进一步努力,按照 cGMP 标准来规范这些产品的制备和组成。